Nephron Pharmaceuticals Corp.: Medical Device Recall in 2013 - (Recall #: Z-1371-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

Product Classification:

Class I

Date Initiated: April 30, 2013

Date Posted: June 5, 2013

Recall Number: Z-1371-2013

Event ID: 65070

Reason for Recall:

Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.

Status: Terminated

Product Quantity: 604 each

Code Information:

Model # EZ-100 Lots # R2029A, R2029B, R2039A, R2042A, R2045A, and R2047A. Atomizer Serial Number Ranges: 1206034476-1206069065 1207003710-1237038299 1207046505-1207081124 1208027421-1208062155 1209000001-1209069179 1209069180-1209069202 1209069203-1209069460 1210000001-1210103680 1210104001-1210104044

Distribution Pattern:

Worldwide Distribution-USA (nationwide) including DC and Puerto Rico and the states of AL, AZ, CA, CO, CT, FL, IL, IN, IO, GA, KS, KY, LA, MD, MN, MS, MO, NK, NV, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN , TX, VT, VA, WA, and WV, and the countries of Guatemala, Poland, Panama, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated